GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3351 - 3375 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0080611
  • anterior segment dysgenesis 6
Homo sapiens (human)
DOID:0080609
  • anterior segment dysgenesis 4
Homo sapiens (human)
DOID:0080608
  • anterior segment dysgenesis 3
Homo sapiens (human)
DOID:0080600
  • COVID-19
  • Aliases:
    • 2019 Novel Coronavirus (2019-nCoV)
    • 2019-nCoV infection
    • COVID19
    • SARS-CoV-2 infection
    • Wuhan coronavirus infection
    • Wuhan seafood market pneumonia virus infection
Homo sapiens (human)
DOID:0080599
  • Coronavirus infectious disease
Homo sapiens (human)
DOID:0080598
  • Kleefstra syndrome 2
Homo sapiens (human)
DOID:0080597
  • Kleefstra syndrome
Homo sapiens (human)
DOID:0080596
  • hyper IgE recurrent infection syndrome 4
Homo sapiens (human)
DOID:0080594
  • hyper IgE recurrent infection syndrome 2
Homo sapiens (human)
DOID:0080592
  • Klippel-Feil syndrome 4
Homo sapiens (human)
DOID:0080591
  • Klippel-Feil syndrome 3
Homo sapiens (human)
DOID:0080589
  • Klippel-Feil syndrome 1
Homo sapiens (human)
DOID:0080588
  • agammaglobulinemia 5
Homo sapiens (human)
DOID:0080586
  • Van Maldergem syndrome 2
Homo sapiens (human)
DOID:0080585
  • Van Maldergem syndrome 1
Homo sapiens (human)
DOID:0080584
  • autosomal dominant Wolfram syndrome
Homo sapiens (human)
DOID:0080582
  • hypotrichosis 14
Homo sapiens (human)
DOID:0080581
  • hyperekplexia 4
Homo sapiens (human)
DOID:0080579
  • 3-Methylcrotonyl-CoA carboxylase 1 deficiency
Homo sapiens (human)
DOID:0080576
  • spondyloepimetaphyseal dysplasia, Genevieve-type
Homo sapiens (human)
DOID:0080573
  • congenital disorder of glycosylation Ix
  • Aliases:
    • congenital disorder of glycosylation 1x
Homo sapiens (human)
DOID:0080572
  • congenital disorder of glycosylation Iw
  • Aliases:
    • congenital disorder of glycosylation 1w
Homo sapiens (human)
DOID:0080571
  • congenital disorder of glycosylation Iu
  • Aliases:
    • congenital disorder of glycosylation 1u
Homo sapiens (human)
DOID:0080553
  • congenital disorder of glycosylation Iaa
  • Aliases:
    • congenital disorder of glycosylation 1aa
Homo sapiens (human)
DOID:0080551
  • Naxos disease
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024